Whittaker G R, Bonass W A, Elton D M, Halliburton I W, Killington R A, Meredith D M
Department of Microbiology, University of Leeds, U.K.
J Gen Virol. 1992 Nov;73 ( Pt 11):2933-40. doi: 10.1099/0022-1317-73-11-2933.
A portion of equine herpesvirus type 1 (EHV-1) gene 28, which is homologous to herpes simplex virus type 1 gene UL32, was expressed using a prokaryotic system to yield a fusion protein which reacted on Western blots with P19, a monoclonal antibody (MAb) that reacts with EHV-1 glycoprotein 300 (gp300), confirming that this gene encodes gp300. Hydrophobicity analysis showed that gp300 is a glycoprotein with multiple hydrophobic domains that might interact with, or span, the membrane several times. As such, it may represent the first member of a new family of herpesvirus glycoproteins to be identified as a virus structural component. Gp300 was also shown to be modified by palmitic acid residues, and a second MAb (1G12) directed against gp300 inhibited fusion between EHV-1-infected cells.
马疱疹病毒1型(EHV-1)基因28的一部分与单纯疱疹病毒1型基因UL32同源,利用原核系统表达该部分基因,产生一种融合蛋白,该融合蛋白在蛋白质免疫印迹法中能与P19发生反应,P19是一种与EHV-1糖蛋白300(gp300)反应的单克隆抗体,证实该基因编码gp300。疏水性分析表明,gp300是一种具有多个疏水结构域的糖蛋白,这些结构域可能与膜相互作用或多次跨越膜。因此,它可能代表了疱疹病毒糖蛋白新家族中第一个被鉴定为病毒结构成分的成员。Gp300还被证明被棕榈酸残基修饰,并且另一种针对gp300的单克隆抗体(1G12)可抑制EHV-1感染细胞之间的融合。